Last updated on June 2019

Denosumab and Nivolumab Combination as 2d-line Therapy in Stage IV NSC Lung Cancer With Bone Metastases (DENIVOS)

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Bone Metastases | Non-Small Cell Lung Cancer
  • Age: Between 18 - 100 Years
  • Gender: Male or Female

Inclusion Criteria:

  • Cytologically or histologically proven stage IV NSCLC
  • Patients who had received first-line platin salt-based chemotherapy and will be given second-line nivolumab;
  • Patients with bone metastases, symptomatic or not, confirmed by X-rays, CT scan, MRI, PET-CT scan or technetium bone scintigraphy
  • Presence of at least 1 measurable target lesion, according to RECIST criteria 1.1, in a non-irradiated site
  • For non-squamous cell NSCLC, patients without activating epidermal growth factor receptor mutation, anaplastic lymphoma kinase (ALK) or reactive oxygen species (ROS)-1 translocation, or BRaf protooncogene, serine/threonine kinase (BRAF V600) mutation
  • PD-L1 status known and expressed as a percentage of tumor cells; assessed at the diagnosis or the more recent PD-L1 expression status available.
  • Eastern Cooperative Oncology Group Performance Status 0/1
  • Estimated life-expectancy 12 weeks
  • No prior malignant tumor during the previous 5 years, except for in situ carcinomas of the cervix or basal or squamous cell carcinomas of the skin adequately treated;
  • Adequate organ function determined by laboratory analyses less than 7 days before
  • Normal hepatic function: bilirubin < 1.5 normal (N), alanine aminotransferase and aspartate aminotransferase <2.5 N or <5 N if hepatic metastases are present
  • Renal function (renal clearance of creatinine at least 45 mL/min)
  • Hematological function: absolute number of neutrophils 1.5109/L and/or platelets 100109/L, hemoglobin 8 g/dL
  • Women of child-bearing age must use an effective contraceptive method and mechanical contraception during and up to 6 months after the end of treatment;
  • Men must use effective contraception during and up to 6 months after the treatment period
  • Subjects with cerebral metastases may be enrolled, provided that all lesions are controlled, and adequately treated by radiotherapy (stereotactic or not), craniotomy, or gamma knife therapy, with no evidence of progression, and have not required steroids for at least 2 months prior to enrolment. Carcinomatous meningitis is excluded regardless of clinical stability
  • Subjects must have signed and dated an approved written informed consent form in accordance with regulatory and institutional guidelines. This must be obtained before the performance of any protocol related procedures that are not part of normal subject care
  • Patient affiliated or benefitting from the French national health insurance program

Exclusion Criteria:

  • Patients previously treated with bisphosphonates and/or denosumab
  • Patients previously treated with immunotherapy
  • Patients with symptomatic cerebral metastases
  • Contraindication to nivolumab use:
  • Prior autoimmune disease(s), define as disease required systemic treatment in the past (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (eg., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment
  • Prior diffuse interstitial pneumopathy
  • Systemic immunosuppressive therapy; define as steroid medication at a dose greater than prednisone 10 mg/day or equivalent. For patients with mismatch repair-deficient high-grade gliomas, concurrent steroid medication at a dose greater than prednisone 20mg/day or equivalent
  • Contraindication for denosumab use:
  • Poor dental status requiring immediate specialized management, like oral surgery
  • Prior or current signs of osteonecrosis of the jaw/osteomyelitis
  • Invasive dental intervention schedule during the study or not yet healed
  • Patient with known sensitivity to any of the products to be administered during the study
  • Concomitant administration of bisphosphonates
  • Hypocalcemia or severe uncorrected hypercalcemia
  • Medical or psychological condition preventing informed consent
  • Pregnant or breastfeeding woman
  • PD-L1-status results unavailable
  • Simultaneous participation of the patient in another clinical research trial

Recruitment Status: Open

Brief Description Eligibility Contact Research Team

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